Use of the Assessment of Caregiver Experience with Neuromuscular Disease (ACEND) in Spinal Muscular Atrophy

被引:0
|
作者
Brown, Laurey [1 ,2 ]
Hoffman, Katie [1 ,2 ]
Corbo-Galli, Chiara [3 ]
Dong, Siyuan [4 ]
Zumpf, Katelyn [4 ]
Weigel, Christa [1 ]
Blomgren, Colleen [1 ]
Munson, Hannah [2 ]
Bidwell, Jessa [2 ]
Rao, Vamshi [2 ,5 ]
Kuntz, Nancy L. [2 ,5 ]
Schwaede, Abigail [2 ]
Krosschell, Kristin J. [5 ,6 ]
机构
[1] Ann & Robert H Lurie Childrens Hosp Chicago, Dept Rehabil Serv, Chicago, IL 60611 USA
[2] Ann & Robert H Lurie Childrens Hosp Chicago, Div Neurol, Chicago, IL 60611 USA
[3] Northwestern Univ, Weinberg Coll Arts & Sci, Evanston, IL 60208 USA
[4] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Div Biostat, Chicago, IL 60611 USA
[5] Northwestern Univ, Feinberg Sch Med, Dept Pediat, Chicago, IL 60611 USA
[6] Northwestern Univ, Feinberg Sch Med, Dept Phys Therapy & Human Movement Sci, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
spinal muscular atrophy; caregiver burden; quality of life; neuromuscular; pediatric; ACEND; FUNCTIONAL MOTOR SCALE; VALIDATION;
D O I
10.3390/jcm13040921
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Spinal muscular atrophy (SMA) has a remarkable impact on function and participation. Subsequently, the caregivers of individuals with SMA are impacted as well. Providers and the SMA community should be aware of the presence of and likely expectations for the existence of caregiver burden. Methods: The Assessment of Caregiver Experience with Neuromuscular Disease (ACEND) quantifies caregivers' perceptions of function and quality of life pertaining to time, finance and emotion. Analyses were conducted among SMA types and ambulatory and ventilatory status. Participants with SMA had varying ranges of function and were on pharmaceutical treatment. Total ACEND score, longitudinal change in total ACEND score, total quality of life (QOL) score, change in total QOL score and subdomains for QOL, including time, emotion and finance, were all explored. Results: Overall, the ACEND demonstrated discriminant validity and some observed trends. Total ACEND scores improved for caregivers of those with SMA 2, remained stable longitudinally for caregivers of those with SMA 1 and 3 and were not influenced by ventilation status. The caregivers of individuals with SMA 1 had the lowest total quality of life (QOL) score, as did the caregivers of non-ambulatory individuals and those requiring assisted ventilation. Longitudinally, there were no changes in total QOL between caregivers of individuals with different SMA types or ambulatory or ventilation status. There were some differences in emotional needs, but no differences in financial impact between the caregivers of individuals with different types of SMA or ambulatory and ventilatory status. Conclusions: With this information enlightening the presence of caregiver burden and expected changes in burden with pharmaceutical treatment, providers, third party payors and the SMA community at large can better assist, equip and empower those providing the necessary assistance to enable the lives of those with SMA.
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页数:15
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